All diseases

OMIM ID
605355
OMIM term:
NEMALINE MYOPATHY 5; NEM5
Alternative terms:
NEMALINE MYOPATHY, AMISH TYPE; ANM
AMISH NEMALINE MYOPATHY
NEMALINE MYOPATHY, CAUSED BY MUTATION IN THE TROPONIN T1 GENE
(∗) Location:
19q13.42  
(†) Associated OMIM genes:
TNNT1  
(‡) Associated MGI genes:

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